Clinical Trial Interim Results Poster Abstract Submission

Present Your Clinical Trial Findings with Confidence

This Clinical Trial Interim Results Poster Abstract Submission template is designed for researchers, principal investigators, and clinical study teams who need to submit interim findings for conference poster sessions. Whether you're presenting at medical conferences, academic symposiums, or research forums, this template streamlines the submission process while ensuring all critical protocol and safety information is captured.

Built for Research Teams and Medical Conferences

Clinical trial poster presentations require precise documentation of study protocols, patient demographics, endpoint data, and regulatory approvals. This template provides a structured format that aligns with standard academic and medical conference requirements, making it easy for research coordinators, clinical investigators, and study managers to compile and submit their interim results efficiently.

Capture Complete Study Information in One Place

The form guides submitters through all essential components of a clinical trial poster abstract: study identification and design, enrollment demographics, primary endpoint results, safety monitoring approvals, and presenter information. With conditional logic built in, the form adapts based on study phase and design, ensuring you only answer relevant questions for your specific trial.

Streamline Conference Submissions with Smart Workflows

Using Paperform's payment features, you can collect conference submission fees directly within the form. Connect your submission data to your research management system via integrations with tools like Airtable, Google Sheets, or your institutional database. For conference organizers, you can use Stepper to automatically route submissions to review committees, send confirmation emails with submission IDs, and track review status across multiple poster categories.

Trusted by Research Institutions and Conference Organizers

This template meets the documentation standards expected by institutional review boards, data safety monitoring boards, and conference scientific committees. The structured format ensures compliance with research presentation guidelines while maintaining the flexibility to accommodate various trial designs and therapeutic areas. Perfect for academic medical centers, pharmaceutical companies, contract research organizations, and professional medical societies hosting poster sessions.